Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
641 | 3217 | 32.5 | 76% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
11 | 4 | NEUROSCIENCES//CLINICAL NEUROLOGY//NEUROL | 1112395 |
653 | 3 | PRION//PRION PROTEIN//CREUTZFELDT JAKOB DISEASE | 11471 |
876 | 2 | PRION//PRION PROTEIN//CREUTZFELDT JAKOB DISEASE | 11471 |
641 | 1 | CREUTZFELDT JAKOB DISEASE//CJD SURVEILLANCE UNIT//PRION DISEASE | 3217 |
Terms with highest relevance score |
rank | Term | termType | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|---|
1 | CREUTZFELDT JAKOB DISEASE | authKW | 4554802 | 22% | 66% | 723 |
2 | CJD SURVEILLANCE UNIT | address | 1198251 | 5% | 77% | 164 |
3 | PRION DISEASE | authKW | 860403 | 9% | 31% | 292 |
4 | CJD | authKW | 453566 | 3% | 54% | 88 |
5 | VARIANT CREUTZFELDT JAKOB DISEASE | authKW | 388608 | 2% | 69% | 59 |
6 | CREUTZFELDT JAKOB DIS SURVEILLANCE UNIT | address | 368942 | 2% | 72% | 54 |
7 | PRION | authKW | 357590 | 9% | 13% | 300 |
8 | GERSTMANN STRAUSSLER SCHEINKER DISEASE | authKW | 324928 | 1% | 80% | 43 |
9 | SPORADIC CREUTZFELDT JAKOB DISEASE | authKW | 324928 | 1% | 80% | 43 |
10 | FATAL FAMILIAL INSOMNIA | authKW | 312859 | 1% | 70% | 47 |
Web of Science journal categories |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | Clinical Neurology | 30609 | 43% | 0% | 1369 |
2 | Neurosciences | 5724 | 26% | 0% | 837 |
3 | Pathology | 5233 | 12% | 0% | 383 |
4 | Medicine, General & Internal | 1179 | 10% | 0% | 333 |
5 | Hematology | 760 | 5% | 0% | 176 |
6 | Neuroimaging | 666 | 2% | 0% | 62 |
7 | Psychiatry | 664 | 6% | 0% | 201 |
8 | Virology | 501 | 4% | 0% | 113 |
9 | Infectious Diseases | 409 | 4% | 0% | 133 |
10 | Public, Environmental & Occupational Health | 159 | 4% | 0% | 139 |
Address terms |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | CJD SURVEILLANCE UNIT | 1198251 | 5% | 77% | 164 |
2 | CREUTZFELDT JAKOB DIS SURVEILLANCE UNIT | 368942 | 2% | 72% | 54 |
3 | CJD SCI TECHNOL | 179285 | 1% | 82% | 23 |
4 | PRION CLIN | 160758 | 1% | 71% | 24 |
5 | MRC PRION UNIT | 156000 | 2% | 34% | 49 |
6 | CENT NERVOUS SYST STUDIES | 147064 | 1% | 50% | 31 |
7 | AUSTRALIAN CREUTZFELDT JAKOB DIS REGISTRY | 139756 | 1% | 82% | 18 |
8 | CNS STUDIES | 125600 | 0% | 88% | 15 |
9 | U360 | 88691 | 1% | 27% | 35 |
10 | REFERENCE TSE SURVEILLANCE | 72996 | 0% | 77% | 10 |
Journals |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | PRION | 23268 | 1% | 7% | 33 |
2 | NEUROLOGY | 15137 | 6% | 1% | 185 |
3 | NEUROPATHOLOGY | 12196 | 1% | 3% | 43 |
4 | FOLIA NEUROPATHOLOGICA | 11452 | 1% | 4% | 32 |
5 | ACTA NEUROPATHOLOGICA | 10580 | 3% | 1% | 81 |
6 | NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY | 7390 | 1% | 2% | 38 |
7 | JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY | 7222 | 3% | 1% | 85 |
8 | ANNALS OF NEUROLOGY | 6932 | 2% | 1% | 76 |
9 | BRAIN PATHOLOGY | 6429 | 1% | 2% | 32 |
10 | NEUROEPIDEMIOLOGY | 4785 | 1% | 2% | 27 |
Author Key Words |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | CREUTZFELDT JAKOB DISEASE | 4554802 | 22% | 66% | 723 | Search CREUTZFELDT+JAKOB+DISEASE | Search CREUTZFELDT+JAKOB+DISEASE |
2 | PRION DISEASE | 860403 | 9% | 31% | 292 | Search PRION+DISEASE | Search PRION+DISEASE |
3 | CJD | 453566 | 3% | 54% | 88 | Search CJD | Search CJD |
4 | VARIANT CREUTZFELDT JAKOB DISEASE | 388608 | 2% | 69% | 59 | Search VARIANT+CREUTZFELDT+JAKOB+DISEASE | Search VARIANT+CREUTZFELDT+JAKOB+DISEASE |
5 | PRION | 357590 | 9% | 13% | 300 | Search PRION | Search PRION |
6 | GERSTMANN STRAUSSLER SCHEINKER DISEASE | 324928 | 1% | 80% | 43 | Search GERSTMANN+STRAUSSLER+SCHEINKER+DISEASE | Search GERSTMANN+STRAUSSLER+SCHEINKER+DISEASE |
7 | SPORADIC CREUTZFELDT JAKOB DISEASE | 324928 | 1% | 80% | 43 | Search SPORADIC+CREUTZFELDT+JAKOB+DISEASE | Search SPORADIC+CREUTZFELDT+JAKOB+DISEASE |
8 | FATAL FAMILIAL INSOMNIA | 312859 | 1% | 70% | 47 | Search FATAL+FAMILIAL+INSOMNIA | Search FATAL+FAMILIAL+INSOMNIA |
9 | PRION PROTEIN | 287674 | 6% | 15% | 200 | Search PRION+PROTEIN | Search PRION+PROTEIN |
10 | VCJD | 268725 | 1% | 60% | 47 | Search VCJD | Search VCJD |
Core articles |
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c: (1) Number of references referring to publications in the class. (2) Share of total number of active references referring to publications in the class. (3) Age of the article. New articles get higher score than old articles. (4) Citation rate, normalized to year. |
Rank | Reference | # ref. in cl. |
Shr. of ref. in cl. |
Citations |
---|---|---|---|---|
1 | LEUCK, CJ , MCILWAINE, GG , ZEIDLER, M , (2000) CREUTZFELDT-JAKOB DISEASE AND THE EYE. I. BACKGROUND AND PATIENT MANAGEMENT.EYE. VOL. 14. ISSUE . P. 263 -290 | 297 | 83% | 0 |
2 | MINIKEL, EV , VALLABH, SM , LEK, M , ESTRADA, K , SAMOCHA, KE , SATHIRAPONGSASUTI, JF , MCLEAN, CY , TUNG, JY , YU, LPC , GAMBETTI, P , ET AL (2016) QUANTIFYING PRION DISEASE PENETRANCE USING LARGE POPULATION CONTROL COHORTS.SCIENCE TRANSLATIONAL MEDICINE. VOL. 8. ISSUE 322. P. - | 99 | 66% | 19 |
3 | TAKADA, LT , KIM, MO , CLEVELAND, RW , WONG, K , FORNER, SA , GALA, II , FONG, JC , GESCHWIND, MD , (2017) GENETIC PRION DISEASE: EXPERIENCE OF A RAPIDLY PROGRESSIVE DEMENTIA CENTER IN THE UNITED STATES AND A REVIEW OF THE LITERATURE.AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. VOL. 174. ISSUE 1. P. 36 -69 | 137 | 81% | 0 |
4 | KOVACS, GG , TRABATTONI, G , HAINFELLNER, JA , IRONSIDE, JW , KNIGHT, RSG , BUDKA, H , (2002) MUTATIONS OF THE PRION PROTEIN GENE - PHENOTYPIC SPECTRUM.JOURNAL OF NEUROLOGY. VOL. 249. ISSUE 11. P. 1567-1582 | 126 | 98% | 134 |
5 | BROWN, K , MASTRIANNI, JA , (2010) THE PRION DISEASES.JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY. VOL. 23. ISSUE 4. P. 277-298 | 137 | 68% | 38 |
6 | LUECK, CJ , MCILWAINE, GG , ZEIDLER, M , (2000) CREUTZFELDT-JAKOB DISEASE AND THE EYE. II. OPHTHALMIC AND NEURO-OPHTHALMIC FEATURES.EYE. VOL. 14. ISSUE . P. 291 -301 | 132 | 92% | 14 |
7 | CHEN, C , DONG, XP , (2016) EPIDEMIOLOGICAL CHARACTERISTICS OF HUMAN PRION DISEASES.INFECTIOUS DISEASES OF POVERTY. VOL. 5. ISSUE . P. - | 73 | 95% | 2 |
8 | MEAD, S , (2006) PRION DISEASE GENETICS.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 14. ISSUE 3. P. 273 -281 | 80 | 95% | 156 |
9 | TAKADA, LT , GESCHWIND, MD , (2013) PRION DISEASES.SEMINARS IN NEUROLOGY. VOL. 33. ISSUE 4. P. 348-356 | 74 | 88% | 7 |
10 | WADSWORTH, JDF , COLLINGE, J , (2007) UPDATE ON HUMAN PRION DISEASE.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1772. ISSUE 6. P. 598 -609 | 96 | 72% | 42 |
Classes with closest relation at Level 1 |